Reaction #79494

ord-bafb5c3f1b15449c9e23e81a8e272203

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe solvent was then evaporated under reduced pressure
  2. 2
    OtherThe residue was purified by column chromatography (ethyl acetate-n-hexane, ⅓)

Procedure

37% hydrochloric acid (5 ml) and water (1 ml) was added at room temperature with stirring to a solution of 4-imino-5-methyl-5-phenyl-3-phenylaminothiazolidine-2-thione (9.38 g) in methanol (50 ml). The solution was stirred for 24 hrs at room temperature. The solvent was then evaporated under reduced pressure. The residue was purified by column chromatography (ethyl acetate-n-hexane, ⅓) to yield an oily 5-methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one (7.02 g).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713629B2uspto-grants-2004_03